A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608951



Internal ID6995875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:49802958..49838775hg38UCSC Ensembl
chr6:49770671..49806488hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3835818
hg1935818
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12345027
SamplesHG03127
Known GenesCRISP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608951
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer